BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GE OEC 9800

    MDR report key: 1033114 · Received April 23, 2008

    Report

    Report Number
    1720753-2008-20842
    Event Type
    Injury
    Date Received
    April 23, 2008
    Date of Event
    April 10, 2008
    Report Date
    April 22, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE REP EVALUATED THE SYS AND REPLACED THE VERTICAL LIFT POWER SUPPLY FUSE. SYS OPERATES AS INTENDED.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THE VERTICAL LIFT ASSEMBLY WILL NOT MOVE UP OR DOWN. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GE OEC 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS 9800 NA

    Patients

    Seq Age Sex Outcome Treatment
    1